Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C33H43FN10O6 |
Molecular Weight | 694.7563 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]1(C[C@@H](O)CN1C(=O)[C@@H](N)CC2=CC=C(F)C=C2)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(=O)N[C@@H](CC3=CNC4=C3C=CC=C4)C(N)=O
InChI
InChIKey=SGXPTOACEHQGHL-RCNLLYRESA-N
InChI=1S/C33H43FN10O6/c34-20-9-7-18(8-10-20)12-23(35)32(50)44-17-21(45)14-27(44)31(49)43-25(6-3-11-39-33(37)38)30(48)41-16-28(46)42-26(29(36)47)13-19-15-40-24-5-2-1-4-22(19)24/h1-2,4-5,7-10,15,21,23,25-27,40,45H,3,6,11-14,16-17,35H2,(H2,36,47)(H,41,48)(H,42,46)(H,43,49)(H4,37,38,39)/t21-,23+,25+,26+,27+/m1/s1
Nemifitide is a peptide analog of melanocyte-inhibiting factor (MIF) that has been reported to relieve depressive symptoms in a very short period. Tetragenex (formerly Innapharma) was developing nemifitide with potential in the treatment of depression. Clinical data obtained from two pilot clinical studies, double-blind, placebo-controlled, parallel-design, in-patient and outpatient, suggested that nemifitide may have the following advantages over current therapies: rapid onset of action (3–5 d), short period of administration (5–10 doses over a 1–2 wk period), and a relatively long duration of treatment effect (3–6 months). The mechanism of action of nemifitide was investigated by evaluating its in-vitro receptor binding and in-vivo localization in the rat brain as well as its interactions with psychoprobes indicative of specific neurotransmitter pathways in acute studies in rats. The results of these studies indicate that nemifitide readily crosses the blood–brain barrier and is localized mainly in the amygdala, hippocampus and frontal cortex of the rat brain. Its in-vitro binding to several receptors including 5-HT-2A, as well as its significant interaction with d-fenfluramine in the rat, suggest the participation of the serotonergic pathway in its mode of action in a different way than that observed with SSRI antidepressants.
CNS Activity
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/12974986
Doses of 18, 36, 54 and 72 mg/d showed almost equal clinical effect of duration between retreatment doses, the 36 mg/d dose being the most reproducible. The range of dose from 18 to 72 mg/d looks promising for the future clinical trials. Nemifitide was administered subcutaneously.
Route of Administration:
Other
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NCI_THESAURUS |
C265
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C90713
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CHEMBL2107761
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DTXSID101336172
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173240-15-8
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8214
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6918348
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RO19OXA9NG
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Nemifitide
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m7800
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PRIMARY | Merck Index |
ACTIVE MOIETY
SALT/SOLVATE (PARENT)